Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100238868-100239220 | Common:1; Rare:130 | ||||
chr14:100239856-100239915 | Rare:10 | ||||
chr14:100375360-100375768 | Common:4; Rare:65 | ||||
chr14:100376236-100376521 | Common:3; Rare:93 | ||||
chr14:100569554-100569662 | Common:1; Rare:24 | ||||
chr14:101809736-101809902 | Rare:34 | ||||
chr14:101964439-101964670 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr14:102038489-102038793 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):6 | ||||
chr14:102083544-102083983 | Common:3; Rare:179 | ||||
chr14:102084398-102085012 | Common:1; Rare:275 | ||||
chr14:102086984-102087306 | Common:4; Rare:130 | ||||
chr14:102139667-102139932 | Rare:93 | ||||
chr14:102305124-102305289 | Common:1; Rare:57 | ||||
chr14:102362847-102363109 | Rare:115 | ||||
chr14:103123215-103123473 | Rare:47 |